Name: rs11453550
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs11453550

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:178799385-178799397 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: delAA / delA / dupA / dupAA / dupA…
delAA / delA / dupA / dupAA / dupAAA
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.2134 (1426/6682, ALFA)
delA=0.2534 (1269/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: AACSP1 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	6682	AAAAAAAAAAAAA=0.6516	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.2134, AAAAAAAAAAAAAA=0.1348, AAAAAAAAAAAAAAA=0.0001, AAAAAAAAAAAAAAAA=0.0000	0.650929	0.110294	0.238777	32
European	Sub	5714	AAAAAAAAAAAAA=0.5933	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.2492, AAAAAAAAAAAAAA=0.1573, AAAAAAAAAAAAAAA=0.0002, AAAAAAAAAAAAAAAA=0.0000	0.571361	0.135109	0.29353	32
African	Sub	528	AAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	24	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	504	AAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	54	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	34	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	20	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	42	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	238	AAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	12	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	94	AAAAAAAAAAAAA=0.96	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.02, AAAAAAAAAAAAAA=0.02, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	0.977778	0.022222	0.0	24

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	6682	(A)₁₃=0.6516	delAA=0.0000, delA=0.2134, dupA=0.1348, dupAA=0.0001, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	5714	(A)₁₃=0.5933	delAA=0.0000, delA=0.2492, dupA=0.1573, dupAA=0.0002, dupAAA=0.0000
Allele Frequency Aggregator	African	Sub	528	(A)₁₃=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	238	(A)₁₃=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Other	Sub	94	(A)₁₃=0.96	delAA=0.00, delA=0.02, dupA=0.02, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Asian	Sub	54	(A)₁₃=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	42	(A)₁₃=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	South Asian	Sub	12	(A)₁₃=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
1000Genomes	Global	Study-wide	5008	(A)₁₃=0.7466	delA=0.2534
1000Genomes	African	Sub	1322	(A)₁₃=0.8427	delA=0.1573
1000Genomes	East Asian	Sub	1008	(A)₁₃=0.7282	delA=0.2718
1000Genomes	Europe	Sub	1006	(A)₁₃=0.6839	delA=0.3161
1000Genomes	South Asian	Sub	978	(A)₁₃=0.662	delA=0.338
1000Genomes	American	Sub	694	(A)₁₃=0.801	delA=0.199

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 5	NC_000005.10:g.178799396_178799397del
GRCh38.p14 chr 5	NC_000005.10:g.178799397del
GRCh38.p14 chr 5	NC_000005.10:g.178799397dup
GRCh38.p14 chr 5	NC_000005.10:g.178799396_178799397dup
GRCh38.p14 chr 5	NC_000005.10:g.178799395_178799397dup
GRCh37.p13 chr 5	NC_000005.9:g.178226397_178226398del
GRCh37.p13 chr 5	NC_000005.9:g.178226398del
GRCh37.p13 chr 5	NC_000005.9:g.178226398dup
GRCh37.p13 chr 5	NC_000005.9:g.178226397_178226398dup
GRCh37.p13 chr 5	NC_000005.9:g.178226396_178226398dup

Gene: AACSP1, acetoacetyl-CoA synthetase pseudogene 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
AACSP1 transcript variant 2	NR_024035.2:n.	N/A	Intron Variant
AACSP1 transcript variant 1	NR_135095.1:n.	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(A)₁₃=	delAA	delA	dupA	dupAA	dupAAA
GRCh38.p14 chr 5	NC_000005.10:g.178799385_178799397=	NC_000005.10:g.178799396_178799397del	NC_000005.10:g.178799397del	NC_000005.10:g.178799397dup	NC_000005.10:g.178799396_178799397dup	NC_000005.10:g.178799395_178799397dup
GRCh37.p13 chr 5	NC_000005.9:g.178226386_178226398=	NC_000005.9:g.178226397_178226398del	NC_000005.9:g.178226398del	NC_000005.9:g.178226398dup	NC_000005.9:g.178226397_178226398dup	NC_000005.9:g.178226396_178226398dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

52 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42506201	Mar 13, 2006 (137)
2	HGSV	ss77943863	Sep 08, 2015 (146)
3	HUMANGENOME_JCVI	ss95415814	Feb 05, 2009 (137)
4	BUSHMAN	ss193839515	Jul 04, 2010 (137)
5	BL	ss256082364	May 09, 2011 (137)
6	PJP	ss295258980	May 09, 2011 (137)
7	SSMP	ss663587173	Apr 01, 2015 (144)
8	1000GENOMES	ss1374928809	Aug 21, 2014 (142)
9	EVA_UK10K_ALSPAC	ss1704995224	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1704995232	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1710247353	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1710247354	Apr 01, 2015 (144)
13	HAMMER_LAB	ss1804227407	Sep 08, 2015 (146)
14	HAMMER_LAB	ss1804227408	Sep 08, 2015 (146)
15	SYSTEMSBIOZJU	ss2626226013	Nov 08, 2017 (151)
16	SWEGEN	ss2998337019	Nov 08, 2017 (151)
17	BEROUKHIMLAB	ss3644201599	Oct 12, 2018 (152)
18	URBANLAB	ss3648241201	Oct 12, 2018 (152)
19	EVA_DECODE	ss3716364968	Jul 13, 2019 (153)
20	EVA_DECODE	ss3716364969	Jul 13, 2019 (153)
21	EVA_DECODE	ss3716364970	Jul 13, 2019 (153)
22	ACPOP	ss3733105823	Jul 13, 2019 (153)
23	ACPOP	ss3733105824	Jul 13, 2019 (153)
24	PACBIO	ss3785340620	Jul 13, 2019 (153)
25	PACBIO	ss3790709845	Jul 13, 2019 (153)
26	PACBIO	ss3795587063	Jul 13, 2019 (153)
27	KHV_HUMAN_GENOMES	ss3807638485	Jul 13, 2019 (153)
28	EVA	ss3829672138	Apr 26, 2020 (154)
29	KOGIC	ss3958285278	Apr 26, 2020 (154)
30	KOGIC	ss3958285279	Apr 26, 2020 (154)
31	KOGIC	ss3958285280	Apr 26, 2020 (154)
32	GNOMAD	ss4135170225	Apr 26, 2021 (155)
33	GNOMAD	ss4135170226	Apr 26, 2021 (155)
34	GNOMAD	ss4135170227	Apr 26, 2021 (155)
35	GNOMAD	ss4135170228	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5175671848	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5175671849	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5175671850	Apr 26, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5267022384	Oct 13, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5267022385	Oct 13, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5267022386	Oct 13, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5267022387	Oct 13, 2022 (156)
43	HUGCELL_USP	ss5464857959	Oct 13, 2022 (156)
44	HUGCELL_USP	ss5464857960	Oct 13, 2022 (156)
45	HUGCELL_USP	ss5464857961	Oct 13, 2022 (156)
46	EVA	ss5508318456	Oct 13, 2022 (156)
47	TOMMO_GENOMICS	ss5713193193	Oct 13, 2022 (156)
48	TOMMO_GENOMICS	ss5713193194	Oct 13, 2022 (156)
49	TOMMO_GENOMICS	ss5713193195	Oct 13, 2022 (156)
50	EVA	ss5836101816	Oct 13, 2022 (156)
51	EVA	ss5836101817	Oct 13, 2022 (156)
52	EVA	ss5855154216	Oct 13, 2022 (156)
53	1000Genomes	NC_000005.9 - 178226386	Oct 12, 2018 (152)
54	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 16854125 (NC_000005.9:178226385::A 939/3854) Row 16854126 (NC_000005.9:178226385:A: 1146/3854)	-	Oct 12, 2018 (152)
55	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 16854125 (NC_000005.9:178226385::A 939/3854) Row 16854126 (NC_000005.9:178226385:A: 1146/3854)	-	Oct 12, 2018 (152)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214122195 (NC_000005.10:178799384::A 33206/132424) Row 214122196 (NC_000005.10:178799384::AA 4776/132542) Row 214122197 (NC_000005.10:178799384::AAA 6/132610)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214122195 (NC_000005.10:178799384::A 33206/132424) Row 214122196 (NC_000005.10:178799384::AA 4776/132542) Row 214122197 (NC_000005.10:178799384::AAA 6/132610)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214122195 (NC_000005.10:178799384::A 33206/132424) Row 214122196 (NC_000005.10:178799384::AA 4776/132542) Row 214122197 (NC_000005.10:178799384::AAA 6/132610)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214122195 (NC_000005.10:178799384::A 33206/132424) Row 214122196 (NC_000005.10:178799384::AA 4776/132542) Row 214122197 (NC_000005.10:178799384::AAA 6/132610)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 214122195 (NC_000005.10:178799384::A 33206/132424) Row 214122196 (NC_000005.10:178799384::AA 4776/132542) Row 214122197 (NC_000005.10:178799384::AAA 6/132610)...	-	Apr 26, 2021 (155)
61	Korean Genome Project Submission ignored due to conflicting rows: Row 14663279 (NC_000005.10:178799385:A: 532/1830) Row 14663280 (NC_000005.10:178799386::A 40/1830) Row 14663281 (NC_000005.10:178799384:AA: 6/1830)	-	Apr 26, 2020 (154)
62	Korean Genome Project Submission ignored due to conflicting rows: Row 14663279 (NC_000005.10:178799385:A: 532/1830) Row 14663280 (NC_000005.10:178799386::A 40/1830) Row 14663281 (NC_000005.10:178799384:AA: 6/1830)	-	Apr 26, 2020 (154)
63	Korean Genome Project Submission ignored due to conflicting rows: Row 14663279 (NC_000005.10:178799385:A: 532/1830) Row 14663280 (NC_000005.10:178799386::A 40/1830) Row 14663281 (NC_000005.10:178799384:AA: 6/1830)	-	Apr 26, 2020 (154)
64	Northern Sweden Submission ignored due to conflicting rows: Row 6390688 (NC_000005.9:178226385:A: 199/586) Row 6390689 (NC_000005.9:178226385::A 101/586)	-	Jul 13, 2019 (153)
65	Northern Sweden Submission ignored due to conflicting rows: Row 6390688 (NC_000005.9:178226385:A: 199/586) Row 6390689 (NC_000005.9:178226385::A 101/586)	-	Jul 13, 2019 (153)
66	8.3KJPN Submission ignored due to conflicting rows: Row 33641155 (NC_000005.9:178226385:A: 4578/16758) Row 33641156 (NC_000005.9:178226385::A 157/16758) Row 33641157 (NC_000005.9:178226385:AA: 2/16758)	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 33641155 (NC_000005.9:178226385:A: 4578/16758) Row 33641156 (NC_000005.9:178226385::A 157/16758) Row 33641157 (NC_000005.9:178226385:AA: 2/16758)	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 33641155 (NC_000005.9:178226385:A: 4578/16758) Row 33641156 (NC_000005.9:178226385::A 157/16758) Row 33641157 (NC_000005.9:178226385:AA: 2/16758)	-	Apr 26, 2021 (155)
69	14KJPN Submission ignored due to conflicting rows: Row 47030297 (NC_000005.10:178799384:A: 7722/28258) Row 47030298 (NC_000005.10:178799384::A 271/28258) Row 47030299 (NC_000005.10:178799384:AA: 2/28258)	-	Oct 13, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 47030297 (NC_000005.10:178799384:A: 7722/28258) Row 47030298 (NC_000005.10:178799384::A 271/28258) Row 47030299 (NC_000005.10:178799384:AA: 2/28258)	-	Oct 13, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 47030297 (NC_000005.10:178799384:A: 7722/28258) Row 47030298 (NC_000005.10:178799384::A 271/28258) Row 47030299 (NC_000005.10:178799384:AA: 2/28258)	-	Oct 13, 2022 (156)
72	UK 10K study - Twins Submission ignored due to conflicting rows: Row 16854125 (NC_000005.9:178226385::A 912/3708) Row 16854126 (NC_000005.9:178226385:A: 1089/3708)	-	Oct 12, 2018 (152)
73	UK 10K study - Twins Submission ignored due to conflicting rows: Row 16854125 (NC_000005.9:178226385::A 912/3708) Row 16854126 (NC_000005.9:178226385:A: 1089/3708)	-	Oct 12, 2018 (152)
74	ALFA	NC_000005.10 - 178799385	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs34430155	May 11, 2012 (137)
rs142559374	May 11, 2012 (137)
rs111280869	May 11, 2012 (137)
rs141249637	May 04, 2012 (137)
rs370328222	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5175671850	NC_000005.9:178226385:AA:	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3716364970, ss3958285280, ss4135170228, ss5267022387, ss5713193195	NC_000005.10:178799384:AA:	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAA	(self)
5741183439	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAA	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss256082364	NC_000005.8:178158991:A:	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss77943863	NC_000005.8:178159003:A:	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
30275607, ss663587173, ss1374928809, ss1704995224, ss1704995232, ss1804227408, ss2626226013, ss2998337019, ss3644201599, ss3733105823, ss3785340620, ss3790709845, ss3795587063, ss3829672138, ss5175671848, ss5836101816	NC_000005.9:178226385:A:	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3648241201, ss3807638485, ss5267022386, ss5464857961, ss5713193193, ss5855154216	NC_000005.10:178799384:A:	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
5741183439	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3716364969, ss3958285278	NC_000005.10:178799385:A:	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss193839515	NT_023133.14:23038060:A:	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss295258980	NC_000005.8:178158998::A	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss1804227407, ss3733105824, ss5175671849, ss5508318456, ss5836101817	NC_000005.9:178226385::A	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss1710247353, ss1710247354	NC_000005.9:178226386::A	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4135170225, ss5267022384, ss5464857959, ss5713193194	NC_000005.10:178799384::A	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
5741183439	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3716364968, ss3958285279	NC_000005.10:178799386::A	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss42506201, ss95415814	NT_023133.13:23037671::A	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4135170226, ss5267022385, ss5464857960	NC_000005.10:178799384::AA	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
5741183439	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4135170227	NC_000005.10:178799384::AAA	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
5741183439	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000005.10:178799384:AAAAAAAAAAA… NC_000005.10:178799384:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs11453550

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs11453550