Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs1470260816

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr7:100071452 (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
T>C
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.000022 (3/137880, GnomAD)
C=0.00039 (11/28258, 14KJPN)
C=0.0005 (3/6404, 1000G_30x) (+ 2 more)
C=0.0020 (9/4470, ALFA)
C=0.0106 (31/2922, KOREAN)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ZNF3 : Synonymous 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 4470 T=0.9980 C=0.0020 0.995973 0.0 0.004027 0
European Sub 4462 T=0.9980 C=0.0020 0.995966 0.0 0.004034 0
African Sub 0 T=0 C=0 0 0 0 N/A
African Others Sub 0 T=0 C=0 0 0 0 N/A
African American Sub 0 T=0 C=0 0 0 0 N/A
Asian Sub 0 T=0 C=0 0 0 0 N/A
East Asian Sub 0 T=0 C=0 0 0 0 N/A
Other Asian Sub 0 T=0 C=0 0 0 0 N/A
Latin American 1 Sub 0 T=0 C=0 0 0 0 N/A
Latin American 2 Sub 0 T=0 C=0 0 0 0 N/A
South Asian Sub 0 T=0 C=0 0 0 0 N/A
Other Sub 8 T=1.0 C=0.0 1.0 0.0 0.0 N/A


Help

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").

Download
Study Population Group Sample Size Ref Allele Alt Allele
gnomAD - Genomes Global Study-wide 137880 T=0.999978 C=0.000022
gnomAD - Genomes European Sub 74930 T=1.00000 C=0.00000
gnomAD - Genomes African Sub 40982 T=0.99995 C=0.00005
gnomAD - Genomes American Sub 13480 T=0.99993 C=0.00007
gnomAD - Genomes Ashkenazi Jewish Sub 3290 T=1.0000 C=0.0000
gnomAD - Genomes East Asian Sub 3090 T=1.0000 C=0.0000
gnomAD - Genomes Other Sub 2108 T=1.0000 C=0.0000
14KJPN JAPANESE Study-wide 28258 T=0.99961 C=0.00039
1000Genomes_30x Global Study-wide 6404 T=0.9995 C=0.0005
1000Genomes_30x African Sub 1786 T=0.9989 C=0.0011
1000Genomes_30x Europe Sub 1266 T=1.0000 C=0.0000
1000Genomes_30x South Asian Sub 1202 T=1.0000 C=0.0000
1000Genomes_30x East Asian Sub 1170 T=1.0000 C=0.0000
1000Genomes_30x American Sub 980 T=0.999 C=0.001
Allele Frequency Aggregator Total Global 4470 T=0.9980 C=0.0020
Allele Frequency Aggregator European Sub 4462 T=0.9980 C=0.0020
Allele Frequency Aggregator Other Sub 8 T=1.0 C=0.0
Allele Frequency Aggregator Latin American 1 Sub 0 T=0 C=0
Allele Frequency Aggregator Latin American 2 Sub 0 T=0 C=0
Allele Frequency Aggregator South Asian Sub 0 T=0 C=0
Allele Frequency Aggregator African Sub 0 T=0 C=0
Allele Frequency Aggregator Asian Sub 0 T=0 C=0
KOREAN population from KRGDB KOREAN Study-wide 2922 T=0.9894 C=0.0106
Help

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 7 NC_000007.14:g.100071452T>C
GRCh37.p13 chr 7 NC_000007.13:g.99669075T>C
Gene: ZNF3, zinc finger protein 3 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
ZNF3 transcript variant 10 NM_001318137.2:c.163+3683…

NM_001318137.2:c.163+3683A>G

 		N/A Intron Variant
ZNF3 transcript variant 14 NM_001371210.1:c.271+3683…

NM_001371210.1:c.271+3683A>G

 		N/A Intron Variant
ZNF3 transcript variant 1 NM_017715.4:c.271+3683A>G N/A Intron Variant
ZNF3 transcript variant 2 NM_032924.5:c.1032A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform 2 NP_116313.3:p.Glu344= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant 11 NM_001362775.2:c.1053A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform 4 NP_001349704.1:p.Glu351= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant 9 NM_001318136.2:c.1053A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform 4 NP_001305065.1:p.Glu351= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant 6 NM_001278291.2:c.924A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform 3 NP_001265220.1:p.Glu308= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant 8 NM_001318135.2:c.1032A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform 2 NP_001305064.1:p.Glu344= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant 13 NM_001362777.2:c.924A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform 3 NP_001349706.1:p.Glu308= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant 12 NM_001362776.2:c.1047A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform 6 NP_001349705.1:p.Glu349= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant 3 NM_001278284.2:c.1032A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform 2 NP_001265213.1:p.Glu344= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant 4 NM_001278287.2:c.1032A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform 2 NP_001265216.1:p.Glu344= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant 7 NM_001278292.2:c.924A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform 3 NP_001265221.1:p.Glu308= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant 22 NM_001371218.1:c.795A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform 7 NP_001358147.1:p.Glu265= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant 21 NM_001371217.1:c.1053A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform 4 NP_001358146.1:p.Glu351= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant 20 NM_001371216.1:c.924A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform 3 NP_001358145.1:p.Glu308= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant 15 NM_001371211.1:c.1032A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform 2 NP_001358140.1:p.Glu344= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant 18 NM_001371214.1:c.1032A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform 2 NP_001358143.1:p.Glu344= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant 19 NM_001371215.1:c.924A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform 3 NP_001358144.1:p.Glu308= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant 16 NM_001371212.1:c.1032A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform 2 NP_001358141.1:p.Glu344= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant 17 NM_001371213.1:c.1032A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform 2 NP_001358142.1:p.Glu344= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant 5 NM_001278290.2:c.1032A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform 2 NP_001265219.1:p.Glu344= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant X7 XM_047420802.1:c.271+3683…

XM_047420802.1:c.271+3683A>G

 		N/A Intron Variant
ZNF3 transcript variant X1 XM_024446919.2:c.1047A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform X1 XP_024302687.1:p.Glu349= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant X2 XM_024446920.2:c.1047A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform X1 XP_024302688.1:p.Glu349= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant X3 XM_024446921.2:c.1047A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform X1 XP_024302689.1:p.Glu349= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant X4 XM_024446925.2:c.939A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform X2 XP_024302693.1:p.Glu313= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant X5 XM_024446928.2:c.939A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform X2 XP_024302696.1:p.Glu313= E (Glu) > E (Glu) Synonymous Variant
ZNF3 transcript variant X6 XM_024446927.2:c.939A>G E [GAA] > E [GAG] Coding Sequence Variant
zinc finger protein 3 isoform X2 XP_024302695.1:p.Glu313= E (Glu) > E (Glu) Synonymous Variant
Help

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
Help

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 T= C
GRCh38.p14 chr 7 NC_000007.14:g.100071452= NC_000007.14:g.100071452T>C
GRCh37.p13 chr 7 NC_000007.13:g.99669075= NC_000007.13:g.99669075T>C
ZNF3 transcript variant 2 NM_032924.5:c.1032= NM_032924.5:c.1032A>G
ZNF3 transcript variant 2 NM_032924.4:c.1032= NM_032924.4:c.1032A>G
ZNF3 transcript variant X5 XM_024446928.2:c.939= XM_024446928.2:c.939A>G
ZNF3 transcript variant X10 XM_024446928.1:c.939= XM_024446928.1:c.939A>G
ZNF3 transcript variant 11 NM_001362775.2:c.1053= NM_001362775.2:c.1053A>G
ZNF3 transcript variant 11 NM_001362775.1:c.1053= NM_001362775.1:c.1053A>G
ZNF3 transcript variant X3 XM_024446921.2:c.1047= XM_024446921.2:c.1047A>G
ZNF3 transcript variant X3 XM_024446921.1:c.1047= XM_024446921.1:c.1047A>G
ZNF3 transcript variant 3 NM_001278284.2:c.1032= NM_001278284.2:c.1032A>G
ZNF3 transcript variant 3 NM_001278284.1:c.1032= NM_001278284.1:c.1032A>G
ZNF3 transcript variant 4 NM_001278287.2:c.1032= NM_001278287.2:c.1032A>G
ZNF3 transcript variant 4 NM_001278287.1:c.1032= NM_001278287.1:c.1032A>G
ZNF3 transcript variant 13 NM_001362777.2:c.924= NM_001362777.2:c.924A>G
ZNF3 transcript variant 13 NM_001362777.1:c.924= NM_001362777.1:c.924A>G
ZNF3 transcript variant 9 NM_001318136.2:c.1053= NM_001318136.2:c.1053A>G
ZNF3 transcript variant 9 NM_001318136.1:c.1053= NM_001318136.1:c.1053A>G
ZNF3 transcript variant X1 XM_024446919.2:c.1047= XM_024446919.2:c.1047A>G
ZNF3 transcript variant X1 XM_024446919.1:c.1047= XM_024446919.1:c.1047A>G
ZNF3 transcript variant X2 XM_024446920.2:c.1047= XM_024446920.2:c.1047A>G
ZNF3 transcript variant X2 XM_024446920.1:c.1047= XM_024446920.1:c.1047A>G
ZNF3 transcript variant 8 NM_001318135.2:c.1032= NM_001318135.2:c.1032A>G
ZNF3 transcript variant 8 NM_001318135.1:c.1032= NM_001318135.1:c.1032A>G
ZNF3 transcript variant 12 NM_001362776.2:c.1047= NM_001362776.2:c.1047A>G
ZNF3 transcript variant 12 NM_001362776.1:c.1047= NM_001362776.1:c.1047A>G
ZNF3 transcript variant X4 XM_024446925.2:c.939= XM_024446925.2:c.939A>G
ZNF3 transcript variant X7 XM_024446925.1:c.939= XM_024446925.1:c.939A>G
ZNF3 transcript variant 5 NM_001278290.2:c.1032= NM_001278290.2:c.1032A>G
ZNF3 transcript variant 5 NM_001278290.1:c.1032= NM_001278290.1:c.1032A>G
ZNF3 transcript variant 7 NM_001278292.2:c.924= NM_001278292.2:c.924A>G
ZNF3 transcript variant 7 NM_001278292.1:c.924= NM_001278292.1:c.924A>G
ZNF3 transcript variant X6 XM_024446927.2:c.939= XM_024446927.2:c.939A>G
ZNF3 transcript variant X9 XM_024446927.1:c.939= XM_024446927.1:c.939A>G
ZNF3 transcript variant 6 NM_001278291.2:c.924= NM_001278291.2:c.924A>G
ZNF3 transcript variant 6 NM_001278291.1:c.924= NM_001278291.1:c.924A>G
ZNF3 transcript variant 21 NM_001371217.1:c.1053= NM_001371217.1:c.1053A>G
ZNF3 transcript variant 15 NM_001371211.1:c.1032= NM_001371211.1:c.1032A>G
ZNF3 transcript variant 17 NM_001371213.1:c.1032= NM_001371213.1:c.1032A>G
ZNF3 transcript variant 22 NM_001371218.1:c.795= NM_001371218.1:c.795A>G
ZNF3 transcript variant 16 NM_001371212.1:c.1032= NM_001371212.1:c.1032A>G
ZNF3 transcript variant 18 NM_001371214.1:c.1032= NM_001371214.1:c.1032A>G
ZNF3 transcript variant 20 NM_001371216.1:c.924= NM_001371216.1:c.924A>G
ZNF3 transcript variant 19 NM_001371215.1:c.924= NM_001371215.1:c.924A>G
zinc finger protein 3 isoform 2 NP_116313.3:p.Glu344= NP_116313.3:p.Glu344=
zinc finger protein 3 isoform X2 XP_024302696.1:p.Glu313= XP_024302696.1:p.Glu313=
zinc finger protein 3 isoform 4 NP_001349704.1:p.Glu351= NP_001349704.1:p.Glu351=
zinc finger protein 3 isoform X1 XP_024302689.1:p.Glu349= XP_024302689.1:p.Glu349=
zinc finger protein 3 isoform 2 NP_001265213.1:p.Glu344= NP_001265213.1:p.Glu344=
zinc finger protein 3 isoform 2 NP_001265216.1:p.Glu344= NP_001265216.1:p.Glu344=
zinc finger protein 3 isoform 3 NP_001349706.1:p.Glu308= NP_001349706.1:p.Glu308=
zinc finger protein 3 isoform 4 NP_001305065.1:p.Glu351= NP_001305065.1:p.Glu351=
zinc finger protein 3 isoform X1 XP_024302687.1:p.Glu349= XP_024302687.1:p.Glu349=
zinc finger protein 3 isoform X1 XP_024302688.1:p.Glu349= XP_024302688.1:p.Glu349=
zinc finger protein 3 isoform 2 NP_001305064.1:p.Glu344= NP_001305064.1:p.Glu344=
zinc finger protein 3 isoform 6 NP_001349705.1:p.Glu349= NP_001349705.1:p.Glu349=
zinc finger protein 3 isoform X2 XP_024302693.1:p.Glu313= XP_024302693.1:p.Glu313=
zinc finger protein 3 isoform 2 NP_001265219.1:p.Glu344= NP_001265219.1:p.Glu344=
zinc finger protein 3 isoform 3 NP_001265221.1:p.Glu308= NP_001265221.1:p.Glu308=
zinc finger protein 3 isoform X2 XP_024302695.1:p.Glu313= XP_024302695.1:p.Glu313=
zinc finger protein 3 isoform 3 NP_001265220.1:p.Glu308= NP_001265220.1:p.Glu308=
zinc finger protein 3 isoform 4 NP_001358146.1:p.Glu351= NP_001358146.1:p.Glu351=
zinc finger protein 3 isoform 2 NP_001358140.1:p.Glu344= NP_001358140.1:p.Glu344=
zinc finger protein 3 isoform 2 NP_001358142.1:p.Glu344= NP_001358142.1:p.Glu344=
zinc finger protein 3 isoform 7 NP_001358147.1:p.Glu265= NP_001358147.1:p.Glu265=
zinc finger protein 3 isoform 2 NP_001358141.1:p.Glu344= NP_001358141.1:p.Glu344=
zinc finger protein 3 isoform 2 NP_001358143.1:p.Glu344= NP_001358143.1:p.Glu344=
zinc finger protein 3 isoform 3 NP_001358145.1:p.Glu308= NP_001358145.1:p.Glu308=
zinc finger protein 3 isoform 3 NP_001358144.1:p.Glu308= NP_001358144.1:p.Glu308=
ZNF3 transcript variant 10 NM_001318137.2:c.163+3683= NM_001318137.2:c.163+3683A>G
ZNF3 transcript variant 14 NM_001371210.1:c.271+3683= NM_001371210.1:c.271+3683A>G
ZNF3 transcript variant 1 NM_017715.3:c.271+3683= NM_017715.3:c.271+3683A>G
ZNF3 transcript variant 1 NM_017715.4:c.271+3683= NM_017715.4:c.271+3683A>G
ZNF3 transcript variant X7 XM_047420802.1:c.271+3683= XM_047420802.1:c.271+3683A>G
Help

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#.

8 SubSNP, 5 Frequency submissions
No Submitter Submission ID Date (Build)
1 GNOMAD ss2747873339 Nov 08, 2017 (151)
2 GNOMAD ss2856796558 Nov 08, 2017 (151)
3 SWEGEN ss3001711669 Nov 08, 2017 (151)
4 KRGDB ss3915277372 Apr 26, 2020 (154)
5 1000G_HIGH_COVERAGE ss5274040907 Oct 13, 2022 (156)
6 EVA ss5375514053 Oct 13, 2022 (156)
7 1000G_HIGH_COVERAGE ss5562826951 Oct 13, 2022 (156)
8 TOMMO_GENOMICS ss5725390546 Oct 13, 2022 (156)
9 1000Genomes_30x NC_000007.14 - 100071452 Oct 13, 2022 (156)
10 gnomAD - Genomes NC_000007.14 - 100071452 Apr 26, 2021 (155)
11 KOREAN population from KRGDB NC_000007.13 - 99669075 Apr 26, 2020 (154)
12 14KJPN NC_000007.14 - 100071452 Oct 13, 2022 (156)
13 ALFA NC_000007.14 - 100071452 Apr 26, 2021 (155)
Help

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).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
22454766, ss2747873339, ss2856796558, ss3001711669, ss3915277372, ss5375514053 NC_000007.13:99669074:T:C NC_000007.14:100071451:T:C (self)
50352886, 270717669, 59227650, 12446302286, ss5274040907, ss5562826951, ss5725390546 NC_000007.14:100071451:T:C NC_000007.14:100071451:T:C (self)
Help

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

No publications for rs1470260816

Help

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.

Software version is: 2.0.1.post820+afb47a3d