Name: rs138450605
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.

rs138450605

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:209836347-209836356 (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: delTT / delT / dupT / dupTT
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.256069 (67779/264690, TOPMED)
delT=0.13439 (1377/10246, ALFA)
delT=0.2366 (1142/4826, 1000G) (+ 4 more)
delT=0.3121 (1359/4354, Estonian)
delTT=0.0049 (19/3854, ALSPAC)
delT=0.1692 (310/1832, Korea1K)
delT=0.30 (12/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: UNC80 : 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	10246	TTTTTTTTTT=0.85965	TTTTTTTT=0.00595, TTTTTTTTT=0.13439, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000	0.771632	0.040695	0.187673	32
European	Sub	7850	TTTTTTTTTT=0.8171	TTTTTTTT=0.0078, TTTTTTTTT=0.1752, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000	0.701346	0.053313	0.245342	32
African	Sub	1618	TTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	72	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1546	TTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	70	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	58	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	12	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	80	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	310	TTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	46	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	272	TTTTTTTTTT=0.993	TTTTTTTT=0.000, TTTTTTTTT=0.007, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000	0.985294	0.0	0.014706	0

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
TopMed	Global	Study-wide	264690	(T)₁₀=0.743931	delT=0.256069
Allele Frequency Aggregator	Total	Global	10246	(T)₁₀=0.85965	delTT=0.00595, delT=0.13439, dupT=0.00000, dupTT=0.00000
Allele Frequency Aggregator	European	Sub	7850	(T)₁₀=0.8171	delTT=0.0078, delT=0.1752, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	1618	(T)₁₀=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	310	(T)₁₀=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	272	(T)₁₀=0.993	delTT=0.000, delT=0.007, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	80	(T)₁₀=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	70	(T)₁₀=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	46	(T)₁₀=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
1000Genomes	Global	Study-wide	4826	(T)₁₀=0.7634	delT=0.2366
1000Genomes	African	Sub	1149	(T)₁₀=0.8790	delT=0.1210
1000Genomes	East Asian	Sub	1007	(T)₁₀=0.8222	delT=0.1778
1000Genomes	Europe	Sub	1003	(T)₁₀=0.6690	delT=0.3310
1000Genomes	South Asian	Sub	977	(T)₁₀=0.698	delT=0.302
1000Genomes	American	Sub	690	(T)₁₀=0.714	delT=0.286
Genetic variation in the Estonian population	Estonian	Study-wide	4354	(T)₁₀=0.6879	delT=0.3121
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(T)₁₀=0.9951	delTT=0.0049
Korean Genome Project	KOREAN	Study-wide	1832	(T)₁₀=0.8308	delT=0.1692
The Danish reference pan genome	Danish	Study-wide	40	(T)₁₀=0.70	delT=0.30

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 2	NC_000002.12:g.209836355_209836356del
GRCh38.p14 chr 2	NC_000002.12:g.209836356del
GRCh38.p14 chr 2	NC_000002.12:g.209836356dup
GRCh38.p14 chr 2	NC_000002.12:g.209836355_209836356dup
GRCh37.p13 chr 2	NC_000002.11:g.210701079_210701080del
GRCh37.p13 chr 2	NC_000002.11:g.210701080del
GRCh37.p13 chr 2	NC_000002.11:g.210701080dup
GRCh37.p13 chr 2	NC_000002.11:g.210701079_210701080dup
UNC80 RefSeqGene	NG_051361.1:g.69431_69432del
UNC80 RefSeqGene	NG_051361.1:g.69432del
UNC80 RefSeqGene	NG_051361.1:g.69432dup
UNC80 RefSeqGene	NG_051361.1:g.69431_69432dup

Gene: UNC80, unc-80 homolog, NALCN channel complex subunit (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
UNC80 transcript variant 3	NM_001371986.1:c.3041+134… NM_001371986.1:c.3041+1345_3041+1346del	N/A	Intron Variant
UNC80 transcript variant 1	NM_032504.2:c.3041+1345_3… NM_032504.2:c.3041+1345_3041+1346del	N/A	Intron Variant
UNC80 transcript variant 2	NM_182587.4:c.3026+1345_3… NM_182587.4:c.3026+1345_3026+1346del	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	(T)₁₀=	delTT	delT	dupT	dupTT
GRCh38.p14 chr 2	NC_000002.12:g.209836347_209836356=	NC_000002.12:g.209836355_209836356del	NC_000002.12:g.209836356del	NC_000002.12:g.209836356dup	NC_000002.12:g.209836355_209836356dup
GRCh37.p13 chr 2	NC_000002.11:g.210701071_210701080=	NC_000002.11:g.210701079_210701080del	NC_000002.11:g.210701080del	NC_000002.11:g.210701080dup	NC_000002.11:g.210701079_210701080dup
UNC80 RefSeqGene	NG_051361.1:g.69423_69432=	NG_051361.1:g.69431_69432del	NG_051361.1:g.69432del	NG_051361.1:g.69432dup	NG_051361.1:g.69431_69432dup
UNC80 transcript variant 3	NM_001371986.1:c.3041+1337=	NM_001371986.1:c.3041+1345_3041+1346del	NM_001371986.1:c.3041+1346del	NM_001371986.1:c.3041+1346dup	NM_001371986.1:c.3041+1345_3041+1346dup
UNC80 transcript variant 1	NM_032504.1:c.3041+1337=	NM_032504.1:c.3041+1345_3041+1346del	NM_032504.1:c.3041+1346del	NM_032504.1:c.3041+1346dup	NM_032504.1:c.3041+1345_3041+1346dup
UNC80 transcript variant 1	NM_032504.2:c.3041+1337=	NM_032504.2:c.3041+1345_3041+1346del	NM_032504.2:c.3041+1346del	NM_032504.2:c.3041+1346dup	NM_032504.2:c.3041+1345_3041+1346dup
UNC80 transcript variant 2	NM_182587.3:c.3026+1337=	NM_182587.3:c.3026+1345_3026+1346del	NM_182587.3:c.3026+1346del	NM_182587.3:c.3026+1346dup	NM_182587.3:c.3026+1345_3026+1346dup
UNC80 transcript variant 2	NM_182587.4:c.3026+1337=	NM_182587.4:c.3026+1345_3026+1346del	NM_182587.4:c.3026+1346del	NM_182587.4:c.3026+1346dup	NM_182587.4:c.3026+1345_3026+1346dup
UNC80 transcript variant X7	XM_005246476.1:c.3041+1337=	XM_005246476.1:c.3041+1345_3041+1346del	XM_005246476.1:c.3041+1346del	XM_005246476.1:c.3041+1346dup	XM_005246476.1:c.3041+1345_3041+1346dup

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#.

54 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GMI	ss288284014	May 04, 2012 (137)
2	1000GENOMES	ss326304403	May 09, 2011 (134)
3	1000GENOMES	ss326323217	May 09, 2011 (134)
4	1000GENOMES	ss326417312	Jan 10, 2018 (151)
5	LUNTER	ss551173448	Apr 25, 2013 (138)
6	LUNTER	ss551243959	Apr 25, 2013 (138)
7	LUNTER	ss552974308	Apr 25, 2013 (138)
8	SSMP	ss663279560	Apr 01, 2015 (144)
9	1000GENOMES	ss1369529961	Aug 21, 2014 (142)
10	1000GENOMES	ss1369529964	Aug 21, 2014 (142)
11	EVA_GENOME_DK	ss1575611775	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1703385059	Jan 10, 2018 (151)
13	EVA_UK10K_TWINSUK	ss1703385115	Jan 10, 2018 (151)
14	EVA_UK10K_ALSPAC	ss1710050708	Apr 01, 2015 (144)
15	EVA_UK10K_TWINSUK	ss1710050711	Apr 01, 2015 (144)
16	HAMMER_LAB	ss1798280587	Sep 08, 2015 (146)
17	HAMMER_LAB	ss1798280590	Sep 08, 2015 (146)
18	JJLAB	ss2030475629	Sep 14, 2016 (149)
19	SWEGEN	ss2991278777	Jan 10, 2018 (151)
20	BIOINF_KMB_FNS_UNIBA	ss3645610687	Oct 11, 2018 (152)
21	EGCUT_WGS	ss3659170572	Jul 13, 2019 (153)
22	EVA_DECODE	ss3705925863	Jul 13, 2019 (153)
23	EVA_DECODE	ss3705925864	Jul 13, 2019 (153)
24	EVA_DECODE	ss3705925865	Jul 13, 2019 (153)
25	ACPOP	ss3729328135	Jul 13, 2019 (153)
26	ACPOP	ss3729328136	Jul 13, 2019 (153)
27	PACBIO	ss3784140022	Jul 13, 2019 (153)
28	PACBIO	ss3789680073	Jul 13, 2019 (153)
29	PACBIO	ss3794553236	Jul 13, 2019 (153)
30	KHV_HUMAN_GENOMES	ss3802385473	Jul 13, 2019 (153)
31	KHV_HUMAN_GENOMES	ss3802385474	Jul 13, 2019 (153)
32	EVA	ss3827480068	Apr 25, 2020 (154)
33	EVA	ss3837159135	Apr 25, 2020 (154)
34	EVA	ss3842580635	Apr 25, 2020 (154)
35	KOGIC	ss3949992858	Apr 25, 2020 (154)
36	GNOMAD	ss4060232286	Apr 27, 2021 (155)
37	GNOMAD	ss4060232287	Apr 27, 2021 (155)
38	GNOMAD	ss4060232288	Apr 27, 2021 (155)
39	GNOMAD	ss4060232289	Apr 27, 2021 (155)
40	TOPMED	ss4542948090	Apr 27, 2021 (155)
41	TOMMO_GENOMICS	ss5156281173	Apr 27, 2021 (155)
42	TOMMO_GENOMICS	ss5156281174	Apr 27, 2021 (155)
43	1000G_HIGH_COVERAGE	ss5251864186	Oct 17, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5251864187	Oct 17, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5251864188	Oct 17, 2022 (156)
46	HUGCELL_USP	ss5451490127	Oct 17, 2022 (156)
47	HUGCELL_USP	ss5451490128	Oct 17, 2022 (156)
48	HUGCELL_USP	ss5451490129	Oct 17, 2022 (156)
49	TOMMO_GENOMICS	ss5687103123	Oct 17, 2022 (156)
50	TOMMO_GENOMICS	ss5687103124	Oct 17, 2022 (156)
51	YY_MCH	ss5803181079	Oct 17, 2022 (156)
52	EVA	ss5821523464	Oct 17, 2022 (156)
53	EVA	ss5821523465	Oct 17, 2022 (156)
54	EVA	ss5852932292	Oct 17, 2022 (156)
55	1000Genomes	NC_000002.11 - 210701071	Oct 11, 2018 (152)
56	The Avon Longitudinal Study of Parents and Children	NC_000002.11 - 210701071	Oct 11, 2018 (152)
57	Genetic variation in the Estonian population	NC_000002.11 - 210701071	Oct 11, 2018 (152)
58	The Danish reference pan genome	NC_000002.11 - 210701071	Apr 25, 2020 (154)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 89508048 (NC_000002.12:209836346::T 5088/139382) Row 89508049 (NC_000002.12:209836346::TT 6/139410) Row 89508050 (NC_000002.12:209836346:T: 35524/139348)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 89508048 (NC_000002.12:209836346::T 5088/139382) Row 89508049 (NC_000002.12:209836346::TT 6/139410) Row 89508050 (NC_000002.12:209836346:T: 35524/139348)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 89508048 (NC_000002.12:209836346::T 5088/139382) Row 89508049 (NC_000002.12:209836346::TT 6/139410) Row 89508050 (NC_000002.12:209836346:T: 35524/139348)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 89508048 (NC_000002.12:209836346::T 5088/139382) Row 89508049 (NC_000002.12:209836346::TT 6/139410) Row 89508050 (NC_000002.12:209836346:T: 35524/139348)...	-	Apr 27, 2021 (155)
63	Korean Genome Project	NC_000002.12 - 209836347	Apr 25, 2020 (154)
64	Northern Sweden Submission ignored due to conflicting rows: Row 2613000 (NC_000002.11:210701070:T: 190/600) Row 2613001 (NC_000002.11:210701070:TT: 8/600)	-	Jul 13, 2019 (153)
65	Northern Sweden Submission ignored due to conflicting rows: Row 2613000 (NC_000002.11:210701070:T: 190/600) Row 2613001 (NC_000002.11:210701070:TT: 8/600)	-	Jul 13, 2019 (153)
66	8.3KJPN Submission ignored due to conflicting rows: Row 14250480 (NC_000002.11:210701070:T: 4167/16760) Row 14250481 (NC_000002.11:210701070::T 1/16760)	-	Apr 27, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 14250480 (NC_000002.11:210701070:T: 4167/16760) Row 14250481 (NC_000002.11:210701070::T 1/16760)	-	Apr 27, 2021 (155)
68	14KJPN Submission ignored due to conflicting rows: Row 20940227 (NC_000002.12:209836346:T: 7075/28256) Row 20940228 (NC_000002.12:209836346::T 1/28256)	-	Oct 17, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 20940227 (NC_000002.12:209836346:T: 7075/28256) Row 20940228 (NC_000002.12:209836346::T 1/28256)	-	Oct 17, 2022 (156)
70	TopMed	NC_000002.12 - 209836347	Apr 27, 2021 (155)
71	UK 10K study - Twins Submission ignored due to conflicting rows: Row 6936383 (NC_000002.11:210701071:T: 1238/3708) Row 6936384 (NC_000002.11:210701070:TT: 18/3708)	-	Apr 25, 2020 (154)
72	UK 10K study - Twins	-	Oct 11, 2018 (152)
73	ALFA	NC_000002.12 - 209836347	Apr 27, 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)
rs796262499	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
6936384, ss1703385059, ss1703385115, ss2991278777, ss3729328136, ss5821523465	NC_000002.11:210701070:TT:	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTT	(self)
ss3705925863, ss4060232289, ss5251864188, ss5451490129	NC_000002.12:209836346:TT:	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTT	(self)
8902864937	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTT	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTT	(self)
ss288284014, ss326304403, ss326323217, ss551173448, ss552974308	NC_000002.10:210409315:T:	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTTT	(self)
12548728, 4908820, 729822, ss663279560, ss1369529961, ss1575611775, ss1798280590, ss2030475629, ss3659170572, ss3729328135, ss3784140022, ss3789680073, ss3794553236, ss3837159135, ss5156281173, ss5821523464	NC_000002.11:210701070:T:	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTTT	(self)
ss1710050708, ss1710050711	NC_000002.11:210701071:T:	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTTT	(self)
6370859, 346770969, ss3645610687, ss3802385474, ss3842580635, ss3949992858, ss4060232288, ss4542948090, ss5251864186, ss5451490127, ss5687103123, ss5803181079, ss5852932292	NC_000002.12:209836346:T:	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTTT	(self)
8902864937	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTTT	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTTT	(self)
ss3705925864	NC_000002.12:209836347:T:	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTTT	(self)
ss326417312, ss551243959	NC_000002.10:210409315::T	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss1798280587, ss3827480068, ss5156281174	NC_000002.11:210701070::T	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss1369529964	NC_000002.11:210701071::T	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss4060232286, ss5251864187, ss5451490128, ss5687103124	NC_000002.12:209836346::T	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTTTTT	(self)
8902864937	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTTTTT	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3802385473	NC_000002.12:209836347::T	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3705925865	NC_000002.12:209836348::T	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss4060232287	NC_000002.12:209836346::TT	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTTTTTT	(self)
8902864937	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTTTTTT	NC_000002.12:209836346:TTTTTTTTTT:… NC_000002.12:209836346:TTTTTTTTTT:TTTTTTTTTTTT	(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 rs138450605

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

rs138450605